ENST00000225964.10:c.4222T>A
MANE Select
|
ENSP00000225964.6:p.Tyr1408Asn
|
|
ENST00000225964.9:c.4222T>A
|
ENSP00000225964.5:p.Tyr1408Asn
|
|
NM_000088.3:c.4222T>A , LRG_1t1:c.4222T>A
|
NP_000079.2:p.Tyr1408Asn
|
|
XM_005257058.3:c.3952T>A
|
XP_005257115.2:p.Tyr1318Asn
|
|
XM_005257059.3:c.3304T>A
|
XP_005257116.2:p.Tyr1102Asn
|
|
XM_011524341.1:c.4024T>A
|
XP_011522643.1:p.Tyr1342Asn
|
|
XM_005257058.4:c.3952T>A
|
XP_005257115.2:p.Tyr1318Asn
|
|
XM_005257059.4:c.3304T>A
|
XP_005257116.2:p.Tyr1102Asn
|
|
NM_000088.4:c.4222T>A
MANE Select
|
NP_000079.2:p.Tyr1408Asn
|
|